The study was devised to evaluate whether it was possible to collect P
hiladelphia-negative precursor cells in patients with chronic myeloid
leukaemia. The approach was based on previous experience showing that
complete remission (Ph-negative bone narrow cells) is rarely achieved
after chemotherapy and is very short-lasting. We decided to explore wh
ether it was possible to collect Ph-negative precursor cells in periph
eral blood during the early phase of haemopoietic recovery. These data
show that: the collection of Ph-negative precursor cells occurred in
12/16 (75%) patients mobilized within one year of diagnosis (group A)
versus 12/33 (36%) in patients with a history of more than one year of
disease (group B). Furthermore the numbers of Ph-negative precursor c
ells were significantly much higher at diagnosis. Ten patients mobiliz
ed at diagnosis were subsequently autografted with such Ph-negative pr
ecursor cells. Five of them remain Ph-negative from 4 to 12 months whi
le the other five have percentages of Ph-positive cells in their marro
w ranging from 20% to 70%. In this stage of the disease the procedure
is safe and associated with a very good compliance. Occasional restora
tion of Ph-negative haemopoiesis could be observed up to 40 months aft
er autograft, in patients of group B, but most of patients revert to P
h-positive haemopoiesis. In conclusion these data suggest that it is p
ossible to restore Ph-negative haemopoieis in 70% of patients mobilize
d at diagnosis. This percentage represent the highest one can obtain w
ithout allogeneic BMT, and this includes patients who never would have
been cytogenetic responders to IFN-alpha. Whether and how long for Ph
-negative status can be maintained is a matter for future observation
and study.